Thalidomide-O-C6-acid
Thalidomide-O-C6-acid Basic information
- Product Name:
- Thalidomide-O-C6-acid
- Synonyms:
-
- Heptanoic acid, 7-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]oxy]-
- Thalidomide 4'-ether-alkylC6-acid
- Thalidomide-O-C6-acid
- BUN 66695
- Thalidomide-O-C6-COOH
- 7-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)oxy)heptanoic acid
- Thalidomide-4-O-C6-COOH
- 7-{[2-(2,6-dioxopiperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]oxy}heptanoic acid
- CAS:
- 2169266-69-5
- MF:
- C20H22N2O7
- MW:
- 402.4
- Mol File:
- 2169266-69-5.mol
Thalidomide-O-C6-acid Chemical Properties
- Boiling point:
- 696.2±55.0 °C(Predicted)
- Density
- 1.390±0.06 g/cm3(Predicted)
- form
- Solid
- pka
- 4.76±0.10(Predicted)
- color
- Off-white to light yellow
Thalidomide-O-C6-acid Usage And Synthesis
Description
BUN 66695, also known as Thalidomide 4'-ether-alkylC6-acid is a cereblon ligand with alkyl linker and terminal acid for onward chemistry. This product has no formal name at the moment.
Uses
Thalidomide-O-C6-COOH is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology[1].
IC 50
Cereblon
storage
Store at -20°C
References
[1] Sato T, et al. Cereblon-Based Small-Molecule Compounds to Control Neural Stem Cell Proliferation in Regenerative Medicine.?Front Cell Dev Biol. 2021;9:629326. Published 2021 Mar 11. DOI:10.3389/fcell.2021.629326
[2] Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-1008. DOI:10.1016/j.cell.2020.07.024
Thalidomide-O-C6-acidSupplier
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Thalidomide-O-C6-acid(2169266-69-5)Related Product Information
- Thalidomide-O-C5-acid
- Thalidomide-4-O-C6-NH2 hydrochloride
- Thalidomide-O-C3-acid
- Thalidomide-O-C10-NH2
- Thalidomide-O-C6-NH2
- Thalidomide-linker 9
- Thalidomide-linker 6
- Thalidomide-O-C6-NH2 TFA
- Pentanoic acid, 5-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]oxy]-
- Propanoic acid, 3-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]oxy]-
- 1H-Isoindole-1,3(2H)-dione, 4-[(7-aminoheptyl)oxy]-2-(2,6-dioxo-3-piperidinyl)-
- Carbamic acid, N-[2-[2-[2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]amino]ethoxy]ethoxy]ethyl]-, 1,1-dimethylethyl ester
- Propanoic acid, 3-[2-[2-[2-[2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]oxy]ethoxy]ethoxy]ethoxy]ethoxy]-
- 4-[(4-Aminobutyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione HCl
- 1H-Isoindole-1,3(2H)-dione, 5-(3-aminopropyl)-2-(2,6-dioxo-3-piperidinyl)-, hydrochloride (1:1)
- Propanoic acid, 3-[2-[2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]oxy]ethoxy]ethoxy]-, 2,5-dioxo-1-pyrrolidinyl ester
- Thalidomide-4-O-C8-NH2
- 5,6-dichloro-2-(2,6-dioxopiperidin-3-yl)-2,3-dihydro-1H-isoindole-1,3-dione